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通过 paired-end 转录组测序对鼻咽癌中的 EBV 基因表达进行全面分析。

Comprehensive profiling of EBV gene expression in nasopharyngeal carcinoma through paired-end transcriptome sequencing.

机构信息

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China.

Department of Experimental Research, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China.

出版信息

Front Med. 2016 Mar;10(1):61-75. doi: 10.1007/s11684-016-0436-0. Epub 2016 Mar 11.

DOI:10.1007/s11684-016-0436-0
PMID:26969667
Abstract

The latent expression pattern of Epstein-Barr Virus (EBV) genes in nasopharyngeal carcinoma (NPC) has been extensively investigated, and the expression of several lytic genes in NPC has been reported. However, comprehensive information through EBV transcriptome analysis in NPC is limited. We performed paired-end RNA-seq to systematically and comprehensively characterize the expression of EBV genes in NPC tissue and C666-1 NPC cell line, which consistently carries EBV. In addition to the transcripts restricted to type II latency infection, the type III latency EBNA3s genes and a substantial number of lytic genes, such as BZLF1, BRLF1, and BMRF1, were detected through RNA-seq and were further verified in C666-1 cells and NPC tissue through realtime PCR.We also performed clustering analysis to classify NPC patient groups in terms of EBV gene expression, which presented two subtypes of NPC samples. Results revealed interesting patterns of EBV gene expression in NPC patients. This clustering was correlated with many signaling pathways, such as those related to heterotrimeric G-protein signaling, inflammation mediated by chemokine and cytokine signaling, ribosomes, protein metabolism, influenza infection, and ECM-receptor interaction. Our combined findings suggested that the expression of EBV genes in NPC is restricted not only to type II latency genes but also to type III latency and lytic genes. This study provided further insights into the potential role of EBV in the development of NPC.

摘要

我们通过 RNA 测序,对 NPC 组织和持续携带 EBV 的 NPC 细胞系 C666-1 中 EBV 基因的表达进行了系统而全面的描述。除了局限于 II 型潜伏感染的转录本外,III 型潜伏 EBVNA3s 基因和大量裂解基因,如 BZLF1、BRLF1 和 BMRF1,通过 RNA 测序检测到,并通过实时 PCR 在 C666-1 细胞和 NPC 组织中进一步验证。我们还进行了聚类分析,根据 EBV 基因表达对 NPC 患者进行分组,结果呈现出两种 NPC 样本亚型。本研究结果揭示了 NPC 患者 EBV 基因表达的有趣模式。这种聚类与许多信号通路相关,如与异三聚体 G 蛋白信号、趋化因子和细胞因子信号介导的炎症、核糖体、蛋白质代谢、流感感染和 ECM-受体相互作用相关的信号通路。我们的综合研究结果表明,NPC 中 EBV 基因的表达不仅局限于 II 型潜伏基因,还局限于 III 型潜伏和裂解基因。本研究进一步深入探讨了 EBV 在 NPC 发展过程中的潜在作用。

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